Early-Onset Pulmonary Events with Combined Brigatinib and Afatinib Treatment of L858/cisT790M/cisC797S NSCLC: A Case Report.

Bing-Jie Lee, Chor-Kuan Lim, Hou-Tai Chang, Jia-Hao Zhang
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Abstract

BACKGROUND Brigatinib is used for anaplastic lymphoma kinase (ALK)-positive lung cancer treatment, and some research showed it was useful in treating triple-mutant epidermal growth factor receptor lung cancer. Clinical trials have shown some potential pulmonary toxicities of brigatinib. The early-onset pulmonary events (EOPEs) of brigatinib are associated with high dosage and older age. The successful treatment of EOPEs with steroids was reported. We present the case of a patient with epidermal growth factor receptor L858R/cis-T790M/cis-C797S triple mutations who developed EOPEs after using brigatinib together with afatinib, and the patient was successfully treated with high-dose steroids. CASE REPORT A 54-year-old woman with underlying stage IV lung adenocarcinoma, ECOG score of 0, was treated with brigatinib and afatinib due to disease progression secondary to L858R/cis-T790M/cis-C797S triple mutations. After starting brigatinib and afatinib, she developed dyspnea and dry cough within 2 days and was intubated due to hypercapnic respiratory failure. The chest X-ray showed bilateral interstitial infiltrates while chest computed tomography (CT) showed bilateral ground-glass opacities. EOPEs were suspected and methylprednisolone was prescribed. The oxygenation of the patient improved and her chest CT showed complete resolution after 2 weeks of steroid treatment. CONCLUSIONS This is the first reported case in which brigatinib combined with afatinib induced EOPEs in a patient with triple-mutant epidermal growth factor receptors of lung cancer. Use of doubled tyrosine kinase inhibitors may result in increased risk of pulmonary toxicities that require high alertness, and the respiratory symptoms should be monitored closely after prescription. The early treatment of EOPEs with high-dose steroids resulted in remarkable improvement.

Abstract Image

Abstract Image

布加替尼和阿法替尼联合治疗L858/ cisc790m /cisC797S NSCLC的早发性肺事件:1例报告
布加替尼用于间变性淋巴瘤激酶(ALK)阳性肺癌的治疗,一些研究表明它对治疗三突变型表皮生长因子受体肺癌有用。临床试验显示布加替尼有一些潜在的肺毒性。布加替尼的早发性肺事件(EOPEs)与高剂量和年龄相关。用类固醇成功治疗EOPEs有报道。我们报告了一例表皮生长因子受体L858R/cis-T790M/cis-C797S三重突变患者,在布加替尼和阿法替尼联合使用后发生EOPEs,并成功使用大剂量类固醇治疗。病例报告:一名54岁女性患有潜在的IV期肺腺癌,ECOG评分为0,由于L858R/cis-T790M/cis-C797S三重突变继发疾病进展,接受布加替尼和阿法替尼治疗。开始布加替尼和阿法替尼治疗后,患者在2天内出现呼吸困难和干咳,并因高碳酸血症性呼吸衰竭而插管。胸部x线示双侧间质浸润,胸部CT示双侧磨玻璃影。怀疑EOPEs,开甲强的松龙。患者的氧合改善,胸部CT显示类固醇治疗2周后完全消退。结论:这是首次报道布加替尼联合阿法替尼在三突变的肺癌表皮生长因子受体患者中诱导EOPEs的病例。使用双酪氨酸激酶抑制剂可能导致肺毒性风险增加,需要高度警惕,处方后应密切监测呼吸道症状。早期使用大剂量类固醇治疗EOPEs可显著改善病情。
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